Evidence map›Paper›PMID 24143237›Full record

ArticlePloS one2013

Imaging the L-type amino acid transporter-1 (LAT1) with Zr-89 immunoPET.

Oluwatayo F Ikotun, Bernadette V Marquez, Chaofeng Huang, Kazue Masuko, Miyamoto Daiji, Takashi Masuko, Jonathan McConathy, Suzanne E Lapi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.9field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Imaging xCT with Immuno-PET in Therapy-Resistant Non-Small Cell Lung Cancer.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
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  6. Preclinical and Clinical Use of Indigenously DevelopedACS pharmacology & translational science · 2023
    Review
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  8. Heteromeric Solute Carriers: Function, Structure, Pathology and Pharmacology.Advances in experimental medicine and biology · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. PET Tracers Beyond FDG in Prostate Cancer.Seminars in nuclear medicine · 2016
    Review
  13. Article
  14. Article
  15. Article
  16. Characterization of 5-(2-F1000Research · 2016
    Article
  17. Article
  18. Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Oluwatayo F IkotunDepartment of Radiology, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Bernadette V Marquez
Chaofeng Huang
Kazue Masuko
Miyamoto Daiji
Takashi Masuko
Jonathan McConathy
Suzanne E Lapi
Washington University in St. Louis · USKindai University · JP

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI David G DeNardo · 2001 to 2026
$128.0M
PET TUMOR AND PROLIFERATION IMAGING VIA CATIONIC AMINO ACID TRANSPORTK08CA154790 · NCI · WASHINGTON UNIVERSITY · PI MCCONATHY, JONATHAN EDWARD · 2011 to 2015
$789k
NCI NIH HHS K08 CA154790NCI NIH HHS K08CA154790NCI NIH HHS P30 CA091842
6 · The paper itself

Abstract

The L-type amino acid transporter-1 (LAT1, SLC7A5) is upregulated in a wide range of human cancers, positively correlated with the biological aggressiveness of tumors, and a promising target for both imaging and therapy. Radiolabeled amino acids such as O-(2-[(18)F]fluoroethyl)-L-tyrosine (FET) that are transport substrates for system L amino acid transporters including LAT1 have met limited success for oncologic imaging outside of the brain, and thus new strategies are needed for imaging LAT1 in systemic cancers. Here, we describe the development and biological evaluation of a novel zirconium-89 labeled antibody, [(89)Zr]DFO-Ab2, targeting the extracellular domain of LAT1 in a preclinical model of colorectal cancer. This tracer demonstrated specificity for LAT1 in vitro and in vivo with excellent tumor imaging properties in mice with xenograft tumors. PET imaging studies showed high tumor uptake, with optimal tumor-to-non target contrast achieved at 7 days post administration. Biodistribution studies demonstrated tumor uptake of 10.5 ± 1.8 percent injected dose per gram (%ID/g) at 7 days with a tumor to muscle ratio of 13 to 1. In contrast, the peak tumor uptake of the radiolabeled amino acid [(18)F]FET was 4.4 ± 0.5 %ID/g at 30 min after injection with a tumor to muscle ratio of 1.4 to 1. Blocking studies with unlabeled anti-LAT1 antibody demonstrated a 55% reduction of [(89)Zr]DFO-Ab2 accumulation in the tumor at 7 days. These results are the first report of direct PET imaging of LAT1 and demonstrate the potential of immunoPET agents for imaging specific amino acid transporters.

Indexed as

Antibodies, MonoclonalRadioisotopesZirconiumAnimalsCell Transformation, NeoplasticHCT116 CellsHeLa CellsHumansIsotope LabelingLarge Neutral Amino Acid-Transporter 1MaleMicePositron-Emission TomographyRatsAntibodies, MonoclonalLarge Neutral Amino Acid-Transporter 1RadioisotopesZirconium

Identifiers

PMID24143237
PMCPMC3797081
OpenAlexW2145038323

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.